Assembly of an Achiral Chromophore into Light‐Responsive Helical Nanostructures in the Absence of Chiral Components

The chirality found in living organisms is one of unsolved mysteries on Earth. It is crucial to understand the manner in which small achiral molecules evolve into helical superstructures in the absence of chiral components because this process can provide important insights regarding the origin of chirality in nature. 1) the uncommon helical assembly of an achiral trigonal chromophore into helical nanostructures with aggregation‐induced emission enhancement (AIEE) characteristics and 2) the tunability of the helical pitch and fluorescence intensity in response to light is reported. The Rietveld refinement of X‐ray diffraction (XRD) patterns and the growth process suggest that a striking transformation from an achiral to an asymmetric molecule can occur as a result of specific interactions with certain solvents, presumably leading to the unique helical assembly. More importantly, exposure to UV or visible light promoted not only the formation of irregular helical structures with a wide range of pitch lengths but also an increase in fluorescence intensity.     

An H2O2 Molecule Stabilized inside Open-Cage C60 Derivatives by a Hydroxy Stopper

An H₂O₂ molecule was isolated inside hydroxylated open-cage fullerene derivatives by mixing an H₂O₂ solution with a precursor molecule followed by reduction of one of carbonyl groups on its orifice. Depending on the reduction site, two structural isomers for H₂O₂@open-fullerenes were obtained. A high encapsulation ratio of 81 % was attained at low temperature. The structures of the peroxosolvate complexes thus obtained were studied by ¹H NMR spectroscopy, X-ray analysis, and DFT calculations, showing strong hydrogen bonding between the encapsulated H₂O₂ and the hydroxy group located at the center of the orifice. This OH group was found to act as a kinetic stopper, and the formation of the hydrogen bonding caused thermodynamic stabilization of the H₂O₂ molecule, both of which prevent its escape from the cage. One of the peroxosolvates was isolated by HPLC, affording H₂O₂@open-fullerene with 100 % encapsulation ratio, likely due to the intramolecular hydrogen-bonding interaction.     

Design and fabrication of bismith-silicate photonic crystal fiber

The process of design and fabrication of bismuth-silicate photonic crystal fiber (Bi-PCF) is reported. The Bi-PCF was fabricated by stack and draw method. This is the first trial of the fabrication of photonic crystal fiber made of bismuth-based glass with stack and draw method. The Bi-PCF structure was designed to reduce group-velocity-dispersion (GVD) in a plausible process. Thermal properties of the glass are investigated to establish the fabrication process. The applying pressure and pumping in fiber preform preparation were effectively utilized to control the air-hole diameter and arrangement. The fabricated Bi-PCF shows the well reduced GVD as the numerical calculation predicted. Fusion splicing between Bi-PCF and SMF-28 was also demonstrated.     

The stability of the modified plane Poiseuille flow in the presence of a transverse magnetic field

The stability against small disturbances of the pressure-driven plane laminar motion of an electrically conducting fluid under a transverse magnetic field is investigated. Assuming that the outer regions adjacent to the fluid layer are electrically non-conducting and not ferromagnetic, the appropriate boundary conditions on the magnetic field perturbations are presented. The Chebyshev collocation method is adopted to obtain the eigenvalue equation, which is then solved numerically. The critical Reynolds number R_c, the critical wave number α_c, and the critical wave speed c_c are obtained for wide ranges of the magnetic Prandtl number P_m and the Hartmann number M. It is found that except for the case when P_m is sufficiently small, the magnetic field has both stabilizing and destabilizing effects on the fluid flow, and that for a fixed value of M the fluid flow becomes more unstable as P_m increases.     

Spectral modulation of higher harmonic spontaneous emission from an optical klystron

Higher harmonics of spontaneous emission from an optical klystron have been observed. The modulation factor of the spontaneous emission spectrum for the higher harmonics can be described by considering the observation system. When the dispersive gap of the optical klystron was fixed, the microstructure interval of the spontaneous emission spectrum at a certain resonant wavelength became narrower as the order of the higher harmonic became larger. Some unique characteristics of the higher harmonics have been clarified, and these studies are likely to contribute to the development of free‐electron lasers using higher harmonics of an optical klystron in the shorter‐wavelengths region.